Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05577689

Novel Therapy Target in Metastatic Prostate Cancer

Combining Multi-omics Analysis and Organoid Models to Search for Novel Therapy Target in Metastatic Prostate Cancer

Status
Recruiting
Phase
Study type
Observational
Enrollment
100 (estimated)
Sponsor
Fudan University · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to use multiomics sequencing to explore the molecular characteristics of metastatic prostate cancer (mPCa), especially metastatic castration-resistant prostate cancer (mCRPC). At the same time, mCRPC models will be constructed, including organoids and animal models, serving as a basic and translational research platform to help identify novel drug targets for mPCa.

Detailed description

Although substantial progress in treatments for prostate cancer have been made in the past decades, distant metastasis and drug resistance remained a major cause of prostate cancer-related deaths. The five-year survival rate for men with mPCa was only 30% and all patients with mPCa would inevitably progress to the castration-resistant stage with limited therapeutic chance. In China, the current situation is more worrying, with rapidly increasing PCa incidence and higher proportion of mPCa diagnosed compared with the Western nations (\~30% vs \~5%). Multiomics sequencing provides a promising strategy to discover the underlying molecular basis driving metastasis and resistance and identify the new treatment strategies for patients with mCRPC. The candidate drug target revealed by the multiomics sequencing could be further examined in the organoid and animal models, facilitating the clinical application from basic discovery. This study can establish a mCRPC research system to find the molecular mechanism and potential intervention targets of mCRPC, thereby paving the way for the discovery of new treatments for mCRPC patients.

Conditions

Interventions

TypeNameDescription
OTHERTissueTissue will be derived from patients during a standard of care procedure

Timeline

Start date
2023-08-01
Primary completion
2026-12-01
Completion
2028-12-01
First posted
2022-10-13
Last updated
2025-06-05

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05577689. Inclusion in this directory is not an endorsement.